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HRID 466364作成日:2026年10月26日

Acetic Acid → N,N-diethyl-N-heptyl-4-[(methylsulfonyl)amino]benzeneethanaminium bromide

https://huagongshe.com/reaction/466364

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Ethyl BromideHCID 6332—
反応物N-(4-Acetyl-2-methylphenyl)methanesulfonamideHCID 19873430—
反応物N-[4-[2-(ethylheptylamino)ethyl]phenyl]methanesulfonamideHCID 53740092—
溶媒AcetonitrileHCID 6342—
生成物N,N-diethyl-N-heptyl-4-[(methylsulfonyl)amino]benzeneethanaminium bromideHCID 19873396—

反応手順

A stirred solution of N-[4-[2-(ethylheptylamino)ethyl]phenyl]methanesulfonamide as prepared in Example 3 (0.332 g, 0.975 mmol) in acetonitrile (3 ml) is treated with HOAc, (0.056 ml, 0.975 mmol) and ethyl bromide (0.73 ml, 9.75 mmol). The solution is refluxed for 1 day, treated with additional ethyl bromide (1 ml) and acetonitrile (3 ml) and refluxed for one additional day. The mixture is concentrated; the residue is mixed with a solution of NaHCO3 (160 mg) in water and extracted with Et2O. The extracts are washed with water, dried (MgSO4) and concentrated to give recovered starting material (0.15 g, identified by TLC). The aqueous layers are combined, made strongly basic with 1N KOH, saturated with potassium bromide and washed with CH2Cl2. The aqueous layer is then acidified with 48% hydrogen bromide and extracted with CH2Cl2. The extracts are washed with saturated potassium bromide, dried (NaSO4) and concentrated to give 0.15 g of N,N-diethyl-N-heptyl-4-[(methylsulfonyl)amino]benzeneethanaminium bromide. MS calc'd for C20H37N2O2S (M+): 369.2576. Found: 369.2585.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05155268
出典データセットuspto-grants-1992_10
ORD IDord-e6e6ab513b7f4085a6d7b165e9cd6194
出典メモuspto-grants-1992_10